1. Immunology/Inflammation Apoptosis
  2. PD-1/PD-L1 Interleukin Related TNF Receptor
  3. Cetrelimab

Cetrelimab  (Synonyms: JNJ 63723283; JNJ 3283)

Cat. No.: HY-P99499 Purity: ≥99.0%
COA

Cetrelimab (JNJ 63723283; JNJ 3283) is a human IgG4κ mAb targeting PD-1. Cetrelimab binds PD-1 (Kd=1.72 nM, HEK293) to block the interaction of PD-1 with PD-L1 and PD-L2 (IC50s=111.7 ng/mL and 138.6 ng/mL, respectively). Cetrelimab stimulates peripheral T cells, increases IFN-γ, IL-2, TNF-α level and inhibits tumor growth in vivo.

For research use only. We do not sell to patients.

CAS No. : 2050478-92-5

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Based on 1 publication(s) in Google Scholar

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Description

Cetrelimab (JNJ 63723283; JNJ 3283) is a human IgG4κ mAb targeting PD-1. Cetrelimab binds PD-1 (Kd=1.72 nM, HEK293) to block the interaction of PD-1 with PD-L1 and PD-L2 (IC50s=111.7 ng/mL and 138.6 ng/mL, respectively). Cetrelimab stimulates peripheral T cells, increases IFN-γ, IL-2, TNF-α level and inhibits tumor growth in vivo[1].

Isotype

Human IgG4 kappa

Recommend Isotype Controls
Species

Human

IC50 & Target

PD-1/PD-L1, PD-1/PD-L2, IFN-γ, IL-2, and TNF-α[1]

In Vitro

Cetrelimab (0.01-30 nM; 5 d) binds to endogenous PD-1 on activated CD4+ and CD8+ T cells with EC50s of 0.16-0.22 µg/mL and 0.17-0.22 µg/mL, respectively[1].
Cetrelimab (0.01-30 μg/mL; 24 h) reverse PD-1-mediated suppression of TCR signaling in Jurkat-PD-1 NFAT reporter cells with CHO-K1 expressing PD-L1[1].
Cetrelimab (0.001-100 nM; 6 d) increases IFN-γ, IL-2, and TNF-α with EC50s of 0.08 ng/mL, 0.07 ng/mL, and 0.02 ng/mL, respectively[1].
Cetrelimab binds to PD-1 in cynomolgus with a Kd value of 0.9 nM[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

In Vivo

Cetrelimab (10 mg/kg; i.p.; single dose) has antitumor efficacy, and decreases tumor volume in PD-1 knock-in (hPD-1KI) mice with MC38 tumor[1].
Cetrelimab (10 mg/kg; i.p.; once every 5 days for 30 d) results significant increases in peripheral blood CD8+ T cells in patient-derived xenograft (PDX) lung model in mice[1].
Cetrelimab (10-100 mg/kg; i.v.; once weekly for 5 weeks) has well tolerance in cynomolgus model[1].
Cetrelimab (0.1-10 mg/kg; i.v.; single dose, monitored for 57 d) shows an nonlinear pharmacokinetics (PK) in cynomolgus, possibly attributable to target-mediated drug deposition (TMDD)[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: hPD-1KI model with mouse PD-1 ECD replaced by the human PD-1 ECD[1]
Dosage: 10 mg/kg
Administration: Intraperitoneal injection; single dose at day 7 after tumor implantation
Result: hPD-1KI mice develop normally and have no immune abnormalities.
Significantly lowered tumor volume at Day 21.
Animal Model: Patient-derived xenograft (PDX) LG1306 lung model in mice[1]
Dosage: 10 mg/kg
Administration: Intraperitoneal injection; every 5 days for 6 cycles
Result: Significantly reduced patient-derived tumor volume by 32%.
Animal Model: Good Laboratory Practice (GLP) toxicity study in cynomolgus[1]
Dosage: 0, 10, 30, or 100 mg/kg
Administration: Intravenous injection; once weekly for 5 weeks
Result: Showed well tolerance in cynomolgus.
Clinical Trial
CAS No.
Appearance

Liquid

Color

Colorless to light yellow

SMILES

[Cetrelimab]

Shipping

Shipping with dry ice.

Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Format
  • Human IgG4 kappa
Biological Activity
  • Immobilized Human PD-1 Protein (ECD, His Tag) can bind Cetrelimab. The EC50 for this effect is 5.75 ng/mL.
Purity & Documentation
References
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Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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